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[ CAS No. 116632-39-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 116632-39-4
Chemical Structure| 116632-39-4
Structure of 116632-39-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 116632-39-4 ]

CAS No. :116632-39-4 MDL No. :MFCD00060664
Formula : C7H6BrI Boiling Point : -
Linear Structure Formula :- InChI Key :GHTUADBHTFHMNI-UHFFFAOYSA-N
M.W : 296.93 Pubchem ID :2724601
Synonyms :

Calculated chemistry of [ 116632-39-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 51.83
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.54
Log Po/w (XLOGP3) : 3.63
Log Po/w (WLOGP) : 3.36
Log Po/w (MLOGP) : 4.25
Log Po/w (SILICOS-IT) : 3.95
Consensus Log Po/w : 3.54

Druglikeness

Lipinski : 1.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -4.46
Solubility : 0.0103 mg/ml ; 0.0000346 mol/l
Class : Moderately soluble
Log S (Ali) : -3.32
Solubility : 0.143 mg/ml ; 0.000481 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.58
Solubility : 0.00786 mg/ml ; 0.0000265 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.96

Safety of [ 116632-39-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 116632-39-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 116632-39-4 ]

[ 116632-39-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 116632-39-4 ]
  • [ 20277-69-4 ]
  • [ 99768-21-5 ]
YieldReaction ConditionsOperation in experiment
With copper(l) iodide; In dimethyl sulfoxide; at 100 - 125℃; for 3.33333h;Microwave irradiation; A mixture of 4-bromo-1-iodo-2-methylbenzene (240 μL, 1.68 mmol, Aldrich), Copper(I) iodide (353 mg, 1.85 mmol, Alfa Aesar), Methanesulfinic acid, sodium salt (688 mg, 6.74 mmol, Alfa Aesar) and DMSO (7.2 mL) was purged with Argon and then heated under microwave condition at 125 C. for 20 min. The resulting mixture was stirred at 100 C. for 3 h and then cooled to room temperature. The reaction mixture was diluted with H2O and extracted with EtOAc (2×). The organic layers were combined and washed with brine, dried over Na2SO4 and concentrated in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 0-50% EtOAc in hexanes) to yield 270 mg of desired product as a white solid. MS (ESI) 249 (M+H).
  • 3
  • [ 116632-39-4 ]
  • [ 105365-51-3 ]
  • [ 1370619-06-9 ]
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